Research Post Vacant @ Syngene | Chem & Pharma Candidates Apply Online

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CAMBRIDGE, UNITED KINGDOM - DECEMBER 09: A scientist lowers biological samples into a liquid nitrogen storage tank at the Cancer Research UK Cambridge Institute on December 9, 2014 in Cambridge, England. Healthy and cancerous biological samples are stored at -196degrees to preserve them for use laboratory tests and experiments. Cancer Research UK is the world's leading cancer charity dedicated to saving lives through research. Its vision is to bring forward the day when all cancers are cured. They have saved millions of lives by discovering new ways to prevent, diagnose and treat cancer, and as such the survival rate in the UK has doubled in the last 40 years. Cancer Research UK funds over 4,000 scientists, doctors and nurses across the UK, more than 33,000 patients who join clinical trials each year and a further 40,000 volunteers that give their time to support the work. (Photo by Dan Kitwood/Getty Images/Cancer Research UK)
Syngene International Limited
Incorporated in the year 1994, Syngene International is one of India premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities. The state-of-the-art research facilities have been qualified by various pharmaceutical majors & regulatory agencies and has received various certifications including ISO 9001: 2008, ISO 14001:2004, OHSAS 18001:2007, GLP and AAALAC.

Job Title:  Senior Research Associate / Senior Associate Scientist

No. of Posts:  1

Job Description:  

Performing the physicochemical and instrumental analysis and investigations of samples. Responsible for handling stability/ Validation activities / method transfers for multiple Client projects & ensuring Qualification and Calibration of assigned Instruments & Equipment.
Responsible for Timely deliverables of projects. Actively participate in Client Audits, regulatory Audits.
To generate and maintain

up to date raw data / records as per applicable procedures. Preparation of lab related procedures, protocols and other quality documents as required. Follow cGMP and company guidelines (Quality and Compliance) in laboratory. Compliance & implementation of quality systems
Review of documents with regard to the physicochemical and instrumental analysis as well as Method transfers carried out for Stability samples according to protocol, Analytical methods, Specifications and procedures

Qualifications:  

  • M. Pharm / M.Sc. Chemistry
  • Expert in Stability. Method transfer and Validation activities.
  • Expert in Handling Analytical instruments.
  • Good Knowledge and experience in GMP environment
  • Able to work independently and make decisions with minimal supervision
  • Good interpersonal skills
  • Good communication skills
  • Good team player

Apply Online

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